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Immunoprophylaxis
Types of immunization Immunoglobulins and vaccines Strategies in vaccine preparation Mechanisms of action of different types of vaccines
NATURAL
Transplacental transfer of IgG Immunity after infection Immunoglobulines in milk (breast feeding) ACTIVE
IMMUNIZATION
Vaccination
ARTIFICIAL (PROPHYLACTIC)
PASSIVE
(Administration of immunoglobulins/antisera)
For prophylaxis or therapy
immediate effect temporary immunity (weeks, months)
Pasive immunization
Antibodies-Immunoglobulins (Ig)
Human immunoglobulins (from blood donors) - human serum (gama)globulin (Ig of various specificity) e.g. for immunodeficiencies... - specific immune globulins (high-titre of specific Ig) e.g. for hepatitis B, tetanus, rabies... Animal (horse) sera (antisera, antitoxins) e.g. for snake venoms, botulism, diphteria... serum disease!!!
Active immunization
(Vaccination)
Primarily for prophylaxis Requires time (weeks) for induction of immune response
Administration
- prior to exposure to pathogen (exception: rabies vaccine) - post-exposure (in combination with specific Ig)
Adjuvant
- increases immunogenicity
Long-lasting immunity
- multiple doses needed for most vaccines
Herd immunity
Vaccine types
Live (attenuated) vaccines - contain live, attenuated (weakend) infectious agents Inactivated (killed) vaccines - contain killed whole infectious agents
Conjugate vaccines - contain T-independent antigen bound to T-dependent antigen Combined (polyvalent) vaccines - contain several antigens of one or more different pathogens New approches for vaccines
Examples
Several viral vaccines (against polio (oral-Sabin), mumps, measles, rubella, varicella) and some bacterial (BCG for tuberculosis)...
Advantages
Induction of both humoral (Abs) and cellular response (CTLs) Long-lasting immunity (administered in one or two doses)
Limitations
Risk in immunocompromised persons Instability (termolabile) BCG (limited efficacy)
Examples
Vaccines against pertussis, typhoid, polio (Salk), influenza...
Advantages
Greater stability Safety (no risk of infection)
Limitations
Low immunogenicity (only Ab induced, adjuvant required) Shorter immunity (multiple, booster administration required)
Examples
Vaccine against pertussis (acellular), tetanus and diphteria (toxoid), influenza (Hemagglutinin and Neuraminidase), hepatitis B (HBsAg) and human papilloma virus (L1 protein) so-called virus-like particles (VLP), pneumococcal and meningococcal polysaccharide vaccines...
Advantages
Same as for inactivated vaccines (greater safety)
Limitations
Same as for inactivated vaccines (lower immunogenecity)
Conjugate vaccines
Principle
Immunization with capsular polysaccharide antigen of one pathogen (weak immunogen in children) conjugated to protein antigen of another pathogen (strong immunogen)
Conjugate vaccines
Principle
Immunization with capsular polysaccharide antigen of one pathogen (weak immunogen in children) conjugated to protein antigen of another pathogen (strong immunogen)
Example
Vaccines against pneumococcus, menigococcus and H. influenzae type B (capsular polysaccharide bound to diptheria toxoid )
Advantages
Same as for subunit vaccines Good immune response to capsular antigens Efficient in children in the first two years of life and asplenic persons
Limitations
Same as for subunit vaccines Relatively high cost
Examples
Vaccines against tetanus, diphtera and pertussis (DTP), measles, mumps and rubella (MMR), polysaccharide or conjugate pneumococcal vaccines...
Advantages
The same as for appropriate single vaccines Good immune response to every component in vaccine Practical (fewer administration, fewer visits of doctor...)
Limitations
Same as for single vaccines
Examples
Ongoing clinical trials for several vaccines (e.g. against HIV)
Advantages
Induction of both humoral (Abs) and cellular immune response (CTLs) Possibility of polyvalent vaccine preparation
Limitations
Repeated administration not possible
Example
Ongoing clinical trials for several pathogens
Advantages
Induction of both humoral (Abs) and cellular immune response (CTLs) Simple handling, possibility of polyvalent vaccines preparation
Limitations
Mechanism of action and possible adverse effects not well understood
1. Example of artificial active immunization is 2. Example of artificial passive immunization is 3. Example of natural active immunization is
a. antigens from different infectious agents b. immunity to tetanus after injection of tetanus toxoid c. immunity to tetanus after injection of antitetanus immunoglobulins